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Volumn 16, Issue 10, 2006, Pages 1073-1076

Abdominal pain related to mitochondrial neurogastrointestinal encephalomyopathy syndrome may benefit from splanchnic nerve blockade

Author keywords

Epigastric pain; Mitochondrial neurogastrointestinal encephalomyopathy; Splanchnic nerve blockade

Indexed keywords

CODEINE; FENTANYL;

EID: 33748754018     PISSN: 11555645     EISSN: 14609592     Source Type: Journal    
DOI: 10.1111/j.1460-9592.2006.01918.x     Document Type: Article
Times cited : (13)

References (9)
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  • 2
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    • Bedlack, R.S.1    Vu, T.2    Hammans, S.3
  • 3
    • 0031681413 scopus 로고    scopus 로고
    • Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome
    • Papadimitriou A, Comi GP, Hadjigeorgiou GM et al. Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome. Neurology 1998; 51: 1086-1092.
    • (1998) Neurology , vol.51 , pp. 1086-1092
    • Papadimitriou, A.1    Comi, G.P.2    Hadjigeorgiou, G.M.3
  • 4
    • 0034096975 scopus 로고    scopus 로고
    • Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations
    • Nishino I, Spinazzola A, Papadimitriou A et al. Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations. Ann Neurol 2000; 47: 792-800.
    • (2000) Ann Neurol , vol.47 , pp. 792-800
    • Nishino, I.1    Spinazzola, A.2    Papadimitriou, A.3
  • 5
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    • Mitochondrial neurogastrointestinal encephalomyopathy syndrome to chromosome 22 q13.32-qter
    • Hirano M, Garcia-de-Yebenes J, Jones AC et al. Mitochondrial neurogastrointestinal encephalomyopathy syndrome to chromosome 22 q13.32-qter. Am J Hum Genet 1998; 63: 526-533.
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    • Hirano, M.1    Garcia-de-Yebenes, J.2    Jones, A.C.3
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    • Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder
    • Hirano M, Silvestri G, Blake DM et al. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder. Neurology 1994; 44: 721-724.
    • (1994) Neurology , vol.44 , pp. 721-724
    • Hirano, M.1    Silvestri, G.2    Blake, D.M.3
  • 7
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    • Diagnosis and management of MNGIE syndrome in children: Case report and review of literature
    • Teitelbaum JE, Berde CB, Nurko S et al. Diagnosis and management of MNGIE syndrome in children: case report and review of literature. J Pediatr Gastroenterol Nutr 2002; 35: 377-383.
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    • Diagnosis and management of mitochondrial diseases
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.